A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192419



Internal ID20759460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39861801..39870300hg38UCSC Ensembl
chr17:38018054..38026553hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498023
Supporting Variants
Samples
Known GenesIKZF3, ZPBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192419
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer